(Q31156092)

18 October 2017

MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data (English)

1 reference

single-nucleotide polymorphism

18 October 2017

1 reference

Mamoru Kato

1

1 reference

18 October 2017

Yusuke Nakamura

series ordinal

2

1 reference

18 October 2017

Tatsuhiko Tsunoda

series ordinal

3

1 reference

18 October 2017

language of work or name

English

0 references

publication date

20 May 2008

1 reference

18 October 2017

1 reference

18 October 2017

24

1 reference

18 October 2017

14

1 reference

18 October 2017

1645-1646

1 reference

A second generation human haplotype map of over 3.1 million SNPs

18 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638261

The population genetics of structural variation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638261

Global variation in copy number in the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638261

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638261

Structural variants: changing the landscape of chromosomes and design of disease studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638261

Algorithms for inferring haplotypes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638261

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2638261

Multiplex PCR-based real-time invader assay (mPCR-RETINA): a novel SNP-based method for detecting allelic asymmetries within copy number variation regions

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18492685

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BIOINFORMATICS/BTN242

1 reference

journals/bioinformatics/KatoNT08

18 October 2017

1 reference

DBLP Dataset 2021-01-02

release_rqjjrfcufjc3lpvc5c5vggnfcq

28 January 2021

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rqjjrfcufjc3lpvc5c5vggnfcq

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

18 October 2017

PubMed publication ID

18492685

1 reference